Zhu Bibo, Ye Jing, Ashraf Usama, Li Yunchuan, Chen Huanchun, Song Yunfeng, Cao Shengbo
State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, Hubei, 430070, P.R China.
Laboratory of Animal Virology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, Hubei, 430070, P.R China.
Sci Rep. 2016 Mar 2;6:22581. doi: 10.1038/srep22581.
MicroRNAs (miRNAs) have been well known to play diverse roles in viral infection at the level of posttranscriptional repression. However, much less is understood about the mechanism by which miRNAs are regulated during viral infection. It is likely that both host and virus contain factors to modulate miRNA expression. Here we report the up-regulation of microRNA-15b (miR-15b) in vitro upon infection with Japanese encephalitis virus (JEV). Analysis of miR-15b precursor, pri-miR-15b and pre-miR-15b, suggest that the regulation occurs transcriptionally. Further, we identified the transcriptional regulatory region of miR-15b that contains consensus binding motif for NF-κB subunit c-Rel and cAMP-response element binding protein (CREB), which are known as transcription factor to regulate gene expression. By promoter fusion and mutational analyses, we demonstrated that c-Rel and CREB bind directly to the promoter elements of miR-15b, which are responsible for miR-15b transcription in response to JEV infection. Finally, we showed that pharmacological inhibition of ERK and NF-κB signaling pathway blocked induction of miR-15b in JEV infection, suggesting important roles of ERK and NF-κB pathway in the regulation of miR-15b gene. Therefore, our observations indicate that induced expression of miR-15b is modulated by c-Rel and CREB in response to JEV infection.
微小RNA(miRNA)在转录后抑制水平上对病毒感染发挥多种作用已广为人知。然而,对于病毒感染期间miRNA的调控机制却知之甚少。宿主和病毒可能都含有调节miRNA表达的因子。在此,我们报告了日本脑炎病毒(JEV)感染后体外微小RNA-15b(miR-15b)的上调。对miR-15b前体、初级miR-15b(pri-miR-15b)和前体miR-15b(pre-miR-15b)的分析表明,这种调控发生在转录水平。此外,我们确定了miR-15b的转录调控区域,该区域包含核因子κB亚基c-Rel和环磷酸腺苷反应元件结合蛋白(CREB)的共有结合基序,它们是已知的调节基因表达的转录因子。通过启动子融合和突变分析,我们证明c-Rel和CREB直接结合到miR-15b的启动子元件上,这些元件负责在JEV感染时miR-15b的转录。最后,我们表明,ERK和NF-κB信号通路的药理抑制作用阻断了JEV感染时miR-15b的诱导,提示ERK和NF-κB通路在miR-15b基因调控中起重要作用。因此,我们的观察结果表明,miR-15b的诱导表达在JEV感染时受c-Rel和CREB的调节。